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3 4 dicqa

Manufactured by Phytolab
Sourced in Germany

3,4-diCQA is a chemical compound that can be used as a reference standard or analytical tool in laboratory settings. It is a chlorogenic acid derivative found in various plant species. The core function of 3,4-diCQA is to serve as a reference material for identification and quantification purposes in analytical research and quality control applications.

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4 protocols using 3 4 dicqa

1

Quantification of Dicaffeoylquinic Acids

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Authentic standards (with the purity of above 99.6%) of dicaffeoylquinic acids (1,3-diCQA, 1,5-diCQA, 3,4-diCQA, 3,5-diCQA, and 4,5-diCQA) were purchased from Phytolab (Vestenbergsgreuth, Germany). Mass spectrometry grade (99.9%) methanol was purchased from Romil Pure Chemistry (Cambridge, UK). Mass spectrometry grade formic acid (with the purity of above 96%) was obtained from Sigma-Aldrich (St. Louis, MO, USA). The analytical column used was a reverse-phase Raptor biphenyl (2.1 × 100 mm, 3 µm) column purchased from Restek (Bellefonte, PA, USA).
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2

Quantifying Dicaffeoylquinic Acid Isomers

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Authentic standards (with the purity of above 99.6%) of trans-dicaffeoylquinic acid (1,3-diCQA, 1,5-diCQA, 3,4-diCQA, 3,5-diCQA, and 4,5-diCQA) were purchased from Phytolab (Vestenbergsgreuth, Germany). Mass spectrometry grade (99.9%) methanol and acetonitrile were obtained from Romil (Cambridge, UK). Mass spectrometry grade formic acid was purchased from Sigma-Aldrich (St. Louis, MO, USA). A UV light box Model CM-10 was purchased from Spectroline (Westbury, NY, USA). Pinnacle, Raptor, Viva, and Ultra columns were purchased from Restek (Bellefonte, PA, USA) and Kinetex columns were purchased from Phenomenex (Torrance, CA, USA). Chromatographic separation was achieved using nine analytical columns: Pinnacle bi-phenyl and C18 (2.1 × 100 mm, 3 µm), Raptor bi-phenyl and C18 (2.1 × 100 mm, 2.7 µm), Viva bi-phenyl (2.1 × 100 mm, 5 µm), Viva C18 (2.1 × 100 mm, 3 µm), Ultra C18 (2.1 × 100 mm, 3 µm), and Kinetex bi-phenyl and phenyl-hexyl (4.6 × 100 mm, 5 µm).
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3

Photochemical Isomerization of Dicaffeoylquinic Acids

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Authentic standards of trans,trans-dicaffeoylquinic acids (1,3-diCQA, 1,5-diCQA, 3,4-diCQA, 3,5-diCQA, and 4,5-diCQA) were purchased from Phytolab (Vestenbergsgreuth, Germany). Analytical grade methanol was purchased from Romil Ltd. (Cambridge, UK). To obtain the cis isomers of the dicaffeoylquinic acids, a 1 mg/ mL stock solution was prepared in 100% methanol. The samples were then irradiated using a UV lamp (Spectroline, USA) operating at 245 nm with an intensity of 390 μW/cm2. The lamp was not covered with any notch filter. The products of UV irradiation were analyzed by liquid chromatography-mass spectrometry,22 (link) and no other species were observed other than those peaks corresponding to the 3,5-diCQA isomers (LC chromatograms shown in Figure S3). For the time-dependent photoisomerization study, the 3,5-diCQA was UV irradiated for 2, 5, 10, 20, 30, 60, and 180 min and the products were analyzed with IMS-MS.
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4

Synthesis and Characterization of Chlorogenic Acids

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3-CQA, 4-CQA, 5-CQA, 3,4-diCQA, 3,5-diCQA and 4,5-diCQA were purchased from Phytolab. Hydroxycinnamic acids standards and acetonitrile (HPLC grade) were purchased from Sigma-Aldrich while formic acid was obtained from Carlo Erba reagent. Not commercially available standards such as feruloylquinic acids (FQAs) and pCoQA were obtained by carrying out their chemical synthesis from condensation reactions between a quinic acid derivative and the corresponding acyl chloride. The identity of these CGAs was confirmed by 1H and 13C NMR spectroscopy (24 , 25 ). Water was treated in a Milli-Q water purification system (Millipore Academic).
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